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the ability to design and manage independent research, analyse and publish complex biological data, and work effectively within a collaborative team environment. An interest in translational science and drug
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expertise. Working closely with NHS partners, you will ensure all research activity meets ethical and regulatory standards while collecting, analysing and presenting high quality data. You will help
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-design workshops, interviews, requirements gathering, data curation/annotation activities, and contribute to the design and evaluation of human–computer interface prototypes through design sprints and
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Interview . Further details and application process For required qualifications, key responsibilities, appointment details, further information about Heriot-Watt, and “how to apply”, please see full advert on
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in participant recruitment and the conduct of in-home, telephone, and online qualitative interviews. The role will also involve making a substantial contribution to qualitative data management and
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Teaching Technicians, Teaching Fellows and AEP equivalent up to and including grade 7. Visit the Centre for Research Staff Development for more information.
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respectful and fair for all. Find out more about the benefits of working at the University and what it is like to live and work in the Durham area on our Why Join Us? - Information Page The Role and
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of human samples collected as part of this clinical trial must comply with the Medicines for Human Use (Clinical Trials) Regulations 2004 and will provide the primary endpoint data that will dictate
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qualitative and quantitative research activities, including ethics applications, data collection and analysis Drafting research documentation such as participant information sheets, consent forms, topic guides
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the research group of Professor Alex Cowan in the Department of Chemistry and the Stephenson Institute for Renewable Energy you will create an integrated platform with comprehensive data logging, enabling